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Biomedical subjects

A S Dabholkar

Publications and source records attributed to A S Dabholkar.

10 recordsLinked to original sources

Regional differences in synaptogenesis in human cerebral cortex.

The formation of synaptic contacts in human cerebral cortex was compared in two cortical regions: auditory cortex (Heschl's gyrus) and prefrontal cortex (middle frontal gyrus). Synapse formation in both cortical regions begins in the fetus, before conceptual age 27 weeks. Synaptic density increases more rapidly in auditory cortex, where the maximum is reached near postnatal age 3 months. Maximum synaptic density in middle frontal gyrus is not reached until after age 15 months. Synaptogenesis occurs concurrently with dendritic and axonal growth and with myelination of the subcortical white matter. A phase of net synapse elimination occurs late in childhood, earlier in auditory cortex, where it has ended by age 12 years, than in prefrontal cortex, where it extends to midadolescence. Synaptogenesis and synapse elimination in humans appear to be heterochronous in different cortical regions and, in that respect, appears to differ from the rhesus monkey, where they are concurrent. In other respects, including overproduction of synaptic contacts in infancy, persistence of high levels of synaptic density to late childhood or adolescence, the absolute values of maximum and adult synaptic density, and layer specific differences, findings in the human resemble those in rhesus monkeys.

Auditory Cortex↗

Ultrastructural changes in the mouse liver induced by hepatotoxin from the freshwater cyanobacterium Microcystis aeruginosa strain 7820.

The time-course of ultrastructural changes was studied in mouse liver hepatocytes after i.p. injection of lethal (100 micrograms/kg) and sublethal (10 micrograms/kg) doses of the heptapeptide hepatotoxin from Microcystis aeruginosa strain 7820, a freshwater blue-green alga (cyanobacterium). At both dose levels the hepatocytes show progressive intracellular changes over time periods of 10, 20, 30, and 60 min. The changes resulting from a lethal dose were more prominent and rapid compared to those of the sublethal dose. The most common responses to lethal and sublethal doses were vesiculation of rough endoplasmic reticulum, swollen mitochondria and degranulation (partial or total loss of ribosomes from vesicles). These vesicles appear to have formed from the dilated parts of rough endoplasmic reticulum by fragmentation or separation. At the lethal dose an increased amount of whorl shaped rough endoplasmic reticulum along with large membrane-bound vacuoles were observed in the cytoplasm. With the sublethal dose an increase in the amount of small and large cytoplasmic lipid droplets occurred. These ultrastructural changes parallel the pathological events which lead to animal death by hemorrhagic shock.

Animals↗

Histochemical studies on the distribution of adenosine triphosphatase and 5'-nucleotidase amongst the constituents of the thoracic ganglia and the associated nerve of Periplaneta americana.

The present study deals with the distribution of adenosine triphosphatase and 5'-nucleotidase in the various constituents of thoracic ganglia and associated nerve of Periplaneta americana. The localization of both the enzymes in the thoracic ganglia is identical. The neural lamella is devoid of any activity for both the enzymes. The ganglion cells are intensely positive at their borders. The neuronal cell surface and/or glial cell processes which envelope the neurons show intense activity for these enzymes. Adenosine triphosphatase and 5'-nucleotidase are present around "giant fibres" and small axons. The activity appears to confine itself in the sheaths. The cytoplasm and the nuclei of the neurons are devoid of enzymatic activity, whereas the nucleoli are slightly active. The nerves are positive for both the enzymes. The role of these enzymes at different sites has also been discussed.

Adenosine Triphosphatases↗